GenPipes Real-life Applications

GenPipes offers several genomic analysis pipelines that can be used for various bioinformatic analyses.

These can be utilized for performing a wide range of standardized and tailored analysis. Following is a brief summary that highlights potential use case for each of the GenPipes Pipelines.

C3G has extensive experience analyzing data from various sequencing applications with state of the art computation methods. It offers various services to next-generation sequencing researchers who wish to use these pipelines for advanced genomic analysis. For customized and case-by-case analysis service, submit your request today.

Following is a summary of real-life application use case for each of the GenPipes Pipelines:

RNA Sequencing

The RNA Sequencing Pipeline helps to quantify transcripts and genes using a reference genome and test for differential expression across experimental conditions. It is also possible to call single nucleotide variants (SNVs), detect fusion gene events and assess alternative splicing events.

De Novo RNA Sequencing

The De Novo RNA Sequencing Pipeline assembles reads to transcripts in the absence of a reference genome, annotates transcripts and tests for differential expression. This is well suited to organisms that are not yet characterized.

miRNA Sequencing

This pipeline can be used to quantify known miRNAs, discovers novel ones using a reference genome and performs differential expression analysis. Additional analysis may include pathway testing, target candidates analysis or miRNA editing.

Pac Bio Genomic Assembly Pipeline

The Pac Bio WGS Pipeline helps to assemble small bacterial to larger genomes sequenced with the Pacific Biosciences technology. Genomes can be polished with Illumina short reads, circularized, called for base modifications and annotated.

DNA Methylation Pipeline

The Methylation Pipeline helps to analyze data coming from bisulfite converted DNA assayed by various sequencing assays such as RRBS, CpG capture, whole genome sequencing or microarrays. Our analysis computes methylation levels and performs differential analysis between experimental conditions.

HiC Pipeline

The HiC Pipeline offers data analysis and provides interaction matrices at several resolutions, compartment analysis, topologically associating domain (TAD) predictions, as well as significant chromosomal interactions. Further analyses may include comparisons across samples/conditions and integration of various sample data (expression data, methylation, CTCF/histone binding sites) with Hi-C data.

Amplicon Sequencing Pipeline

The Amplicon Sequencing Pipeline can process Illumina, PacBio pyrotags amplicons from the 16S, 18S or ITS amplicons. OTUs are picked and diversity is analyzed within and between communities. Further analyses include differential abundance testing or metagenome functional content prediction.

DNA Sequencing

The DNA Sequencing Pipeline offers state of the art DNA-seq analyses detects and annotates variants in whole exomes, whole genomes or high coverage amplicons. The analysis can also be pushed further by assisting with variant prioritization, or perform advanced cancer related analysis.

ChIP Sequencing Pipeline

The ChIP Sequencing Pipeline helps in analyzing DNA fragments from immunoprecipitated chromatin by calling alignment peaks on the genome, annotating the said peaks and performing additional analyses such as motif enrichment and discovery. Designed experiments can be analyzed by testing for differential binding between experimental conditions.